JPS606979B2 - oil collecting material - Google Patents

oil collecting material

Info

Publication number
JPS606979B2
JPS606979B2 JP10077373A JP10077373A JPS606979B2 JP S606979 B2 JPS606979 B2 JP S606979B2 JP 10077373 A JP10077373 A JP 10077373A JP 10077373 A JP10077373 A JP 10077373A JP S606979 B2 JPS606979 B2 JP S606979B2
Authority
JP
Japan
Prior art keywords
oil
surfactant
water
filament
polypropylene
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP10077373A
Other languages
Japanese (ja)
Other versions
JPS5051485A (en
Inventor
敏彦 鬼武
是則 小林
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsui Petrochemical Industries Ltd
Original Assignee
Mitsui Petrochemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsui Petrochemical Industries Ltd filed Critical Mitsui Petrochemical Industries Ltd
Priority to JP10077373A priority Critical patent/JPS606979B2/en
Publication of JPS5051485A publication Critical patent/JPS5051485A/ja
Publication of JPS606979B2 publication Critical patent/JPS606979B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は、界面活性剤を配合したポリオレフィンを素材
とする油補集材に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an oil scavenger made of polyolefin containing a surfactant.

近年産業の発達に伴って石油の消費量が増加すると同時
に、それによる環境汚染が進み大きな社会問題となって
いる。
In recent years, with the development of industry, the consumption of petroleum has increased, and at the same time, environmental pollution has progressed and become a major social problem.

たとえばタンカーから排出されるバラスト水、ビジル水
あるいは工場排水等に含まれる油すなわち脂肪族炭化水
素、芳香族炭化水素、脂環式炭化水素(これらの炭化水
素類はS、N、0などを含んだへテロ化合物となってい
てもよい)などからなる石油系炭化水素による海洋、河
川等の汚染がそれである。海面や河川水面に浮遊してい
る油を除くため、あるいは工場排水中の油を除去するた
め、種々の油補集材の開発研究がなされている。
For example, oils contained in ballast water, vital water, or factory wastewater discharged from tankers, such as aliphatic hydrocarbons, aromatic hydrocarbons, and alicyclic hydrocarbons (these hydrocarbons include S, N, 0, etc.) An example of this is the pollution of oceans, rivers, etc. by petroleum-based hydrocarbons, which may be heterogeneous compounds. In order to remove oil floating on the sea surface or river water surface, or to remove oil from industrial wastewater, research and development are being conducted on the development of various oil scavenging materials.

このような油補集素材として、安価でしかも親油性の高
いポリオレフィンが注目されているが未だ総集速度、橋
集量等の橋集性能は充分とは言い難い。したがって工場
排水中の油のように、比較的油濃度の低い汚水を処理し
て、たとえば油を1肋以下にするというような高度の油
総集能を期待することはできなかった。一方、油との相
溶性の大きい素材は横集性能が良好ではあるが、油に対
する溶解性が強いため、たとえば繊維状にして充填塔に
つめ油を含む汚水を通過せしめると、油を捕集するにつ
れ繊維間の粘着や繊維の膨潤により、ついには目詰りを
起し水の通過を妨げるようになって長期の運転ができな
くなる。また特殊な油が流入すると橘集材そのものが溶
解することもある。従って大容量の排水処理を連続的に
行なうというような目的には適していない。本発明の目
的は、油補集能の改善されたボリオレフィン系油補集材
を提供するにある。
Although polyolefins, which are inexpensive and have high lipophilic properties, are attracting attention as such oil scavenging materials, their cross-collection performance such as overall collection speed and amount of cross-collection is still far from satisfactory. Therefore, it was not possible to expect a high level of oil concentration, such as treating wastewater with a relatively low oil concentration, such as oil in factory wastewater, to reduce the amount of oil to less than one cell. On the other hand, materials with high compatibility with oil have good horizontal collection performance, but because they have a strong solubility in oil, if they are made into fibers and passed through a packed tower, for example, they will collect oil. As time goes on, the fibers stick together and the fibers swell, eventually causing clogging and impeding the passage of water, making long-term operation impossible. In addition, when a special oil flows in, the Tachibana wood itself may dissolve. Therefore, it is not suitable for the purpose of continuously treating large volumes of wastewater. An object of the present invention is to provide a polyolefin oil scavenger with improved oil scavenging ability.

本発明の他の目的は、比較的油濃度の低い汚水を処理し
た場合に、油含有量を1脚以下にすることが可能な高性
能の油補集材を提供することにある。本発明のさらに他
の目的は、充填塔などに充填して大量の排水処理を行っ
ても、長期間にわたって連続運転が可能な油補集熊大な
る油構築材を提供することにある。本発明によれば腸イ
オン界面活性剤または陰イオン界面活性剤をポリオレフ
ィンに0.1ないし2重量%配合した油補集材が提供さ
れる。
Another object of the present invention is to provide a high-performance oil scavenger that can reduce the oil content to one foot or less when treating wastewater with a relatively low oil concentration. Still another object of the present invention is to provide an oil collecting material that can be operated continuously for a long period of time even when it is packed into a packed tower or the like to treat a large amount of wastewater. According to the present invention, an oil scavenger is provided in which 0.1 to 2% by weight of an ionic surfactant or an anionic surfactant is blended with a polyolefin.

本発明で用いられるポリオレフィンはポリエチレン、ポ
リプロピレン、ポリ−1ーブデン、ポリー4ーメチル−
1−ペンテン、エチレン・プロピレン共重合体などであ
る。
The polyolefins used in the present invention are polyethylene, polypropylene, poly-1-butene, poly-4-methyl-
1-pentene, ethylene/propylene copolymer, etc.

このうちもっとも適しているのはアイソタクチツクポリ
プロピレンである。ポリオレフィンに配合される界面活
性剤としては陽イオン型または陰イオン型が選択される
Of these, isotactic polypropylene is most suitable. A cationic or anionic surfactant is selected as the surfactant to be blended with the polyolefin.

陽イオン界面活性剤としてはラウリルアミン塩酸塩のよ
うな高級アルキルアミンの塩、セチルピリジニウムク。
リド、アルキルトリメチルアンモニウムプロミド、アル
キルジメチルアンモニウムクロリドのような第四アンモ
ニウム塩を例示することができる。また陰イオン界面活
性剤としては高級カルボン酸塩、高級アルコールの硫酸
ェステル塩、スルホン酸塩などが使用できる。これら界
面活性剤の使用量はポリオレフィンと界面活性剤の合計
量に対し0.1ないし2.の重量%とくに0.2なし、
し1.の重量%の範囲が好ましい。
Examples of cationic surfactants include higher alkylamine salts such as laurylamine hydrochloride, and cetylpyridinium salts.
Examples include quaternary ammonium salts such as chloride, alkyltrimethylammonium bromide, and alkyldimethylammonium chloride. Further, as the anionic surfactant, higher carboxylate salts, higher alcohol sulfate ester salts, sulfonate salts, etc. can be used. The amount of these surfactants used is 0.1 to 2.0% based on the total amount of polyolefin and surfactant. % by weight, especially 0.2,
1. A range of % by weight is preferred.

界面活性剤の使用量を過度に増やしても増量効果が現れ
ないのみならず、繊維状に成形する場合には糸切れの恐
れがでてくるので前記のような範囲にするのが好ましい
。界面活性剤をポリオレフィンに配合するにはバンバリ
ーミキサー、熱ロール、押出機などを用いることによっ
て行なわれる。
If the amount of surfactant used is increased too much, not only will the effect of increasing the amount not be obtained, but also there is a risk of thread breakage when forming into a fiber, so it is preferable to keep it within the above range. The surfactant is blended into the polyolefin using a Banbury mixer, hot roll, extruder, or the like.

このような界面活性剤配合のポリオレフィンを油補集村
として使用する場合、発泡体、ビーズ状その他の形態が
考えられるが、もっと好ましいのは繊維状物の集合体、
加工体たとえば綿、繊維東、織物、不織布などの形態で
ある。このような形態では繊維素材の吸着能と、繊維、
繊維間の空隙に粘性と凝縮性により油を保持する能力の
両者が働き多量の油を綾集処理できるからである。した
がってたとえば充填容器に、繊維あるいは不織布などを
充填して油構築装置を作る場合、単綴維の繊度1ないし
20デニール、好ましくは2なし、し15デニールのも
のを充填密度0.1ないし0.4夕/地、好ましくは0
.1なし、し0.2夕/洲になるように充填するのがよ
い。以下、実施例により説明する。
When such surfactant-containing polyolefin is used as an oil scavenger, it may be in the form of foam, beads, or other shapes, but more preferably it is an aggregate of fibrous materials,
The processed material may be in the form of cotton, textiles, woven fabrics, non-woven fabrics, etc. In this form, the adsorption capacity of the fiber material and the fiber,
This is because both the viscosity and the ability to retain oil in the spaces between the fibers work together, allowing a large amount of oil to be collected. Therefore, for example, when making an oil construction device by filling a filling container with fibers or non-woven fabric, single fibers with a fineness of 1 to 20 deniers, preferably 2 to 15 deniers, are used at a packing density of 0.1 to 0. 4 evenings/earth, preferably 0
.. It is best to fill the tank so that the amount is 1% and 0.2 times per month. Examples will be explained below.

実施例 1 ポリプロピレン(商品名 三井石油化学ポリプロ;アイ
ソタクチツクポリプロピレン、M『R24夕/10hi
n:ASTMD12父山、密度0.91夕/塊:AST
MD1505)に陽イオン界面活性剤テトラデシルジメ
チルベンジルアンモニウムクロリド(商品名 ニツサン
カチオンM−100)を配合したものを溶融紙糸し、5
デニールのフィラメントを得た。
Example 1 Polypropylene (trade name: Mitsui Petrochemical Polypropylene; Isotactic Polypropylene, M'R24/10hi
n: ASTMD12 Chiyama, density 0.91 evening/clump: AST
MD1505) and the cationic surfactant tetradecyldimethylbenzyl ammonium chloride (trade name Nitsusan Cation M-100) were blended into melt paper threads.
I got a denier filament.

C重油771脚を含有する水500ccとフィラメント
1夕を振とう器(1そ分液ロート)に入れ40分間上下
に振とう(振幅30〜4枕肋、振動回数120回/分)
させた後、フィラメントを除去し、水中に残留している
C重油を測定した。
Put 500 cc of water containing 771 legs of C heavy oil and 1 night of filament into a shaker (1 separator funnel) and shake it up and down for 40 minutes (amplitude 30-4 diaphragms, number of vibrations 120 times/min).
After that, the filament was removed and the C heavy oil remaining in the water was measured.

結果を第1表に示す。尚水中のC重油濃度はJISKO
I02、24へキサン抽出法により測定した。
The results are shown in Table 1. The concentration of heavy oil C in water is determined by JISKO.
Measured by I02,24 hexane extraction method.

第 1 表陽イオン界面活性剤を配合したものは、無配
合品にくらべて残留油濃度が低下し(すなわち油補集量
が増加した)、フィラメント間の粘着も見受けられなか
った。
Table 1: In the products containing a cationic surfactant, the residual oil concentration was lower (that is, the amount of oil collected was increased) compared to the product without the addition of a cationic surfactant, and no adhesion between filaments was observed.

実施例 2 ポリプロピレン(商品名 三井石油化学ポリプロ;アイ
ソタクチツクポリプロピレン、MmR24夕/1瓜hi
n:ASTN D123礼、密度0.91夕/塊:AS
TMD1505)に陰イオン界面活性剤ラゥリルアルコ
ール硫酸ヱステルのナトリウム塩(商品名ェマール10
)を配合したものを溶融紙糸し、57ニールのフィラメ
ントを得た。
Example 2 Polypropylene (trade name: Mitsui Petrochemical Polypropylene; Isotactic Polypropylene, MmR24/1-hi
n: ASTN D123, density 0.91 evening/clump: AS
TMD1505) and the anionic surfactant lauryl alcohol sulfate sodium salt (trade name: EMAR 10).
) was blended into a molten paper yarn to obtain a filament of 57 niels.

C重油82劫血を含有する水500ccとフィラメント
1夕を実施例1と同様に振とう器に入れ40分間振とう
ごせた後フィラメントを除去し、水中に残留しているC
重油を実施例1と同様に測定した。
500 cc of water containing 82 tons of C heavy oil and 1 liter of filament were placed in a shaker in the same manner as in Example 1, and after shaking for 40 minutes, the filament was removed and the C remaining in the water was removed.
Heavy oil was measured in the same manner as in Example 1.

結果を第2表に示す。第 2 表 陰イオン界面活性剤を配合したものは、無配合品にくら
べて残留油濃度が低下し(すなわち油補集量が増加した
)、フィラメント間の粘着も見受けられなかった。
The results are shown in Table 2. Table 2: The anionic surfactant-containing product had a lower residual oil concentration (that is, the amount of oil collected increased) than the product without the anionic surfactant, and no adhesion between filaments was observed.

実施例 3〜6 実施例1におけるポリプロピレン及びテトラデシルジメ
チルベンジルアンモニウムクロリドの代わりに第3表に
示すポリオレフインと界面活性剤を用い、実施例1と同
様に5デニールのフィラメントを溶融紙糸した。
Examples 3 to 6 In the same manner as in Example 1, 5-denier filaments were made into fused paper yarns using the polyolefins and surfactants shown in Table 3 instead of the polypropylene and tetradecyldimethylbenzyl ammonium chloride in Example 1.

C重油を第3表に示す濃度で含有する水(原水)500
ccとフィラメント1夕を振とう器に入れ、あとは実施
例1と同様にした。
Water containing C heavy oil at the concentration shown in Table 3 (raw water) 500
cc and one filament were placed in a shaker, and the rest was carried out in the same manner as in Example 1.

水中に残留しているC重油濃度の測定結果を第3表に示
す。第 3 表1)MFR24g/10肌:AST’
の U 1238K準し26000荷重5Kgで測定、
密度0.835gイめ:AST1・4 D 15052
)MFR6.5g/10のの:AS町M ○12388
密度0.91gえめ:ASTM D 15053)実施
例1と同じポリプロピレン4)ェフコ−ル■o、松本油
旨社製 5)マーボマ−セ■。
Table 3 shows the measurement results of the C heavy oil concentration remaining in the water. Table 3 1) MFR24g/10 skin: AST'
Measured at 26000 load 5kg according to U 1238K,
Density 0.835g: AST1・4 D 15052
) MFR6.5g/10: AS Town M ○12388
Density: 0.91 g Material: ASTM D 15053) Same polypropylene as in Example 1 4) Fefcol ■o, manufactured by Matsumoto Yuji Co., Ltd. 5) Marbomerce ■.

T、松本油脂社製実施例7〜8および比較例1 実施例1と同じポリプロピレンに腸イオン界面活性剤と
してテトラデシルジメチルベンジルアンモニゥムクロリ
ドまたは陰イオン界面活性剤としてラゥリルアルコール
硫酸ェステルのナトリウム塩を1.0重量%配合したも
のあるいは界面活性剤を配合しないものを溶融紡糸し、
5デニールのフイラメントを得た。
T, manufactured by Matsumoto Yushi Co., Ltd. Examples 7 to 8 and Comparative Example 1 The same polypropylene as in Example 1 was added with tetradecyldimethylbenzyl ammonium chloride as an ionic surfactant or sodium lauryl alcohol sulfate ester as an anionic surfactant. Melt-spun a product containing 1.0% salt or no surfactant,
A filament of 5 denier was obtained.

このフィラメントを内径64肌の円筒槽内に高さ30肌
、充填密度0.13タ′地で充填し、C重油濃度4朝風
の原水を線速度2比ネ/minで流し、経過時間毎の処
理水油分濃度及び圧損を測定した。
This filament was packed in a cylindrical tank with an inner diameter of 64 mm, a height of 30 mm, and a packing density of 0.13 mm, and raw water of C heavy oil concentration 4 in Asakaze was flowed at a linear velocity of 2 min/min. The treated water oil concentration and pressure drop were measured.

結果を第4表に示す。第 4 表 実施例9〜10および比較例2 ポリプロピレンの代わりに実施例3のポリ山4ーメチル
−1ーベンテンを用いるほかは実施例9〜10および比
較例1と同様に行った。
The results are shown in Table 4. Table 4 Examples 9 to 10 and Comparative Example 2 The same procedures as Examples 9 to 10 and Comparative Example 1 were carried out except that polyyama 4-methyl-1-bentene of Example 3 was used instead of polypropylene.

結果を第5表に示す。第 5 表 これらの結果を見ても判るとおり、油分濃度が40〜5
0個程度の比較的低いものを処理すると、15畑時間近
く連続処理しても処理水の油分濃度は1脚以下であり、
また繊維の膨欄もなく庄損も小さく、たとえば14錨時
間通水後の圧損は無配合品に比べ半分以下なので少なく
とも無配合品に比べ倍以上の連続処理が可能である。
The results are shown in Table 5. Table 5 As you can see from these results, the oil concentration was between 40 and 5.
If a relatively low number of about 0 is treated, the oil concentration in the treated water will be less than 1 foot even after continuous treatment for nearly 15 hours,
In addition, there is no swelling of the fibers, and the erosion loss is small, for example, the pressure loss after passing water for 14 hours is less than half that of a non-blended product, so it is possible to carry out continuous processing at least twice as long as a non-blended product.

実施例11〜12及び比較例3〜4 実施例1と同じポリプロピレンに陽イオン界面活性剤と
してテトラデシルメチルベンジルアンモニウムクロリド
または陰イオン界面活性剤としてラウリルアルコール硫
酸ェステルのナトリウム塩または非イオン界面活性剤と
してポリオキシェチレンノニルフエノ−ルエーテル(H
LB13.3)または両性イオン界面活性剤としてジメ
チルアルキル(ャシ)べタインを1.の重量%配合した
ものを溶融紙糸し、5デニールのフィラメントを得た。
Examples 11-12 and Comparative Examples 3-4 The same polypropylene as in Example 1, tetradecylmethylbenzylammonium chloride as a cationic surfactant, or sodium salt of lauryl alcohol sulfate ester or a nonionic surfactant as an anionic surfactant. as polyoxyethylene nonyl phenol ether (H
LB13.3) or dimethylalkyl(basic) betaine as a zwitterionic surfactant. A 5-denier filament was obtained by melt-melting paper yarn containing 5 denier filament.

このフィラメントを内径64柳の円筒槽内に高さ30功
、充填密度0.13夕/めで充填し、C重油濃度4則血
の原水を線速度20伽′mjnで流し、経過時間毎の処
理水油分濃度及び圧損を測定した。結果を第6表に示す
。第 6 表 これらの結果を見ても判るとおり、陽イオン界面活性剤
および陰イオン界面活性剤は処理を開始すると直ちに含
油水中の油が橘集されて処理水の油濃度が減少するのに
対して、非イオン界面活性剤および両性イオン界面活性
剤は処理開始直後の油補集能力は小さくて、処理水の油
濃度はそれ程減少しない。
This filament was packed into a cylindrical tank made of willow with an inner diameter of 64 mm at a height of 30 mm and a packing density of 0.13 m/m, and raw water with a C heavy oil concentration of 4 standard blood was flowed at a linear velocity of 20 mjn, and treatment was performed at each elapsed time. Water-oil concentration and pressure drop were measured. The results are shown in Table 6. Table 6 As can be seen from these results, cationic surfactants and anionic surfactants cause the oil in the oil-containing water to collect as soon as the treatment starts, reducing the oil concentration in the treated water. Therefore, nonionic surfactants and zwitterionic surfactants have a small oil scavenging ability immediately after the start of treatment, and the oil concentration of the treated water does not decrease significantly.

Claims (1)

【特許請求の範囲】[Claims] 1 陽イオン界面活性剤または陰イオン界面活性剤を0
.1ないし2重量%配合したポリオレフインからなるこ
とを特徴とする油捕集材。
1 0 cationic surfactant or anionic surfactant
.. An oil-trapping material characterized by comprising 1 to 2% by weight of polyolefin.
JP10077373A 1973-09-08 1973-09-08 oil collecting material Expired JPS606979B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10077373A JPS606979B2 (en) 1973-09-08 1973-09-08 oil collecting material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10077373A JPS606979B2 (en) 1973-09-08 1973-09-08 oil collecting material

Publications (2)

Publication Number Publication Date
JPS5051485A JPS5051485A (en) 1975-05-08
JPS606979B2 true JPS606979B2 (en) 1985-02-21

Family

ID=14282791

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10077373A Expired JPS606979B2 (en) 1973-09-08 1973-09-08 oil collecting material

Country Status (1)

Country Link
JP (1) JPS606979B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1303828C (en) * 1987-02-09 1992-06-23 Thomas Irvin Bair Article for absorbing liquids
JP5244474B2 (en) * 2008-06-27 2013-07-24 株式会社東芝 Functional particles and water treatment method using the same

Also Published As

Publication number Publication date
JPS5051485A (en) 1975-05-08

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